NDC 82338-438 Benjamins Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 82338 - P. A Benjamin Manufacturing Co Ltd
- 82338-438 - Benjamins Hand Sanitizer
Product Characteristics
Product Packages
NDC Code 82338-438-24
Package Description: 240 mL in 1 BOTTLE, PUMP
NDC Code 82338-438-38
Package Description: 3800 mL in 1 BOTTLE, PLASTIC
NDC Code 82338-438-60
Package Description: 60 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 82338-438?
What are the uses for Benjamins Hand Sanitizer?
Which are Benjamins Hand Sanitizer UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Benjamins Hand Sanitizer Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- POGOSTEMON CABLIN LEAF OIL (UNII: F3IN55X5PO)
- HYDROXYISOHEXYL 3-CYCLOHEXENE CARBOXALDEHYDE (UNII: QUE43B9Z2Q)
- DIHYDROMYRCENOL (UNII: 46L1B02ND9)
- GRAPEFRUIT OIL (UNII: YR377U58W9)
- 2-ISOBUTYL-4-METHYLTETRAHYDROPYRAN-4-OL (UNII: VK5ZHH2T3F)
- ETHYL LINALOOL (UNII: SF2JS9GF5T)
- 3-(3,4-METHYLENEDIOXYPHENYL)-2-METHYLPROPANAL (UNII: L65EG8H6PA)
- BENZYL SALICYLATE (UNII: WAO5MNK9TU)
- 3-HEXENYL SALICYLATE, CIS- (UNII: C78Y9OR6YH)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- WATER (UNII: 059QF0KO0R)
- CARBOMER 940 (UNII: 4Q93RCW27E)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- TROLAMINE (UNII: 9O3K93S3TK)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ETHYLENE BRASSYLATE (UNII: 9A87HC7ROD)
- ISOCYCLEMONE E (UNII: 1GD7ODM28Y)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- LINALYL ACETATE (UNII: 5K47SSQ51G)
- BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
- .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
- METHYL DIHYDROJASMONATE (SYNTHETIC) (UNII: 3GW44CIE3Y)
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".